Pioglitazone (7.5 mg/day) added to flutamide-metformin in women with androgen excess: additional increments of visfatin and high molecular weight adiponectin

Clin Endocrinol (Oxf). 2008 Feb;68(2):317-20. doi: 10.1111/j.1365-2265.2007.03137.x. Epub 2007 Nov 19.

Abstract

Background and aim: Low-dose pioglitazone (Pio), flutamide (Flu), metformin (Met) plus an oestro-progestagen is a novel polytherapy lowering total and visceral adiposity, and reducing carotid intima media thickness (IMT) in hyperinsulinaemic women with androgen excess, without changing their body mass index (BMI). In a search for mediators of PioFluMet's actions, we measured serum levels of visfatin and high molecular weight (HMW) adiponectin.

Design and patients: In a double-blind study, we enrolled 38 young women with hyperinsulinaemic androgen excess [mean BMI: 23.7 kg/m(2)], all of whom started on Flu (62.5 mg/day), Met (850 mg/day) and a transdermal oestro-progestagen, each for 21/28 days over 1 year. Patients were randomly assigned to receive, in addition, placebo (n = 19) or Pio (7.5 mg/day; n = 19) on the same 21/28 days.

Measurements: Serum concentrations of visfatin and HMW adiponectin, visceral fat by magnetic resonance imaging, carotid IMT by ultrasound, all carried out during study start and after 1 year.

Results: PioFluMet raised visfatin by a mean 84% and HMW adiponectin by 157% (P < 0.001), and reduced visceral fat and IMT by a mean 22% and 31% (both P < 0.001). Low-dose Pio accounted for about half of the PioFluMet effects on IMT, visfatin and HMW adiponectin.

Conclusion: In hyperinsulinaemic women with androgen excess, low-dose polytherapy with PioFluMet evoked striking rises in both circulating visfatin and HMW adiponectin, while lowering IMT and reducing visceral adiposity within 1 year.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adiponectin / metabolism*
  • Adolescent
  • Adult
  • Double-Blind Method
  • Female
  • Flutamide / therapeutic use*
  • Humans
  • Hyperandrogenism / blood
  • Hyperandrogenism / drug therapy*
  • Hyperinsulinism / drug therapy*
  • Metformin / therapeutic use*
  • Nicotinamide Phosphoribosyltransferase / blood
  • Nicotinamide Phosphoribosyltransferase / therapeutic use*
  • Pioglitazone
  • Thiazolidinediones / therapeutic use*
  • Young Adult

Substances

  • Adiponectin
  • Thiazolidinediones
  • Flutamide
  • Metformin
  • Nicotinamide Phosphoribosyltransferase
  • Pioglitazone